Dictionary:
e·las·to·mer (ĭ-lăs'tə-mər) ![]() |
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| Chemistry Dictionary: elastomer |
A natural or synthetic rubber or rubberoid material, which has the ability to undergo deformation under the influence of a force and regain its original shape once the force has been removed.
| Computer Desktop Encyclopedia: elastomer |
(ELASTic pOlyMER) A soft, compliant, rubber-like material.
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| Dental Dictionary: elastomer |
A soft, rubberlike material; synthetic rubber. A rubber base impression material (for example, silicone, mercaptan).
| Architecture: elastomer |
A macromolecular material (such as rubber or a synthetic material having similar properties) that returns rapidly to approximately the initial dimensions and shape after substantial deformation by a weak stress and release of the stress.
| Columbia Encyclopedia: elastomer |
| Wikipedia: Elastomer |
| This article includes a list of references, related reading or external links, but its sources remain unclear because it lacks inline citations. Please improve this article by introducing more precise citations where appropriate. (September 2008) |
An elastomer is a polymer with the property of elasticity. The term, which is derived from elastic polymer, is often used interchangeably with the term rubber, although the latter is preferred when referring to vulcanisates. Each of the monomers which link to form the polymer is usually made of carbon, hydrogen, oxygen and/or silicon. Elastomers are amorphous polymers existing above their glass transition temperature, so that considerable segmental motion is possible. At ambient temperatures rubbers are thus relatively soft (E~3MPa) and deformable. Their primary uses are for seals, adhesives and molded flexible parts.
Elastomers are usually thermosets (requiring vulcanization) but may also be thermoplastic (see thermoplastic elastomer). The long polymer chains cross-link during curing, i.e., vulcanizing. The molecular structure of elastomers can be imagined as a 'spaghetti and meatball' structure, with the meatballs signifying cross-links. The elasticity is derived from the ability of the long chains to reconfigure themselves to distribute an applied stress. The covalent cross-linkages ensure that the elastomer will return to its original configuration when the stress is removed. As a result of this extreme flexibility, elastomers can reversibly extend from 5-700%, depending on the specific material. Without the cross-linkages or with short, uneasily reconfigured chains, the applied stress would result in a permanent deformation.
Temperature effects are also present in the demonstrated elasticity of a polymer. Elastomers that have cooled to a glassy or crystalline phase will have less mobile chains, and consequentially less elasticity, than those manipulated at temperatures higher than the glass transition temperature of the polymer.
It is also possible for a polymer to exhibit elasticity that is not due to covalent cross-links, but instead for thermodynamic reasons.
Unsaturated rubbers that can be cured by sulfur vulcanization:
(Note that unsaturated rubbers can also be cured by non-sulfur vulcanization if desired).
Saturated Rubbers that cannot be cured by sulfur vulcanization:
Various other types of elastomers:
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
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